Active Ingredient: AMPHOTERICIN B
Proprietary Name: AMPHOTERICIN B
Dosage Form; Route of Administration: INJECTABLE, LIPOSOMAL; INJECTION
Strength: 50MG/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A212514
Product Number: 001
Approval Date: Dec 14, 2021
Applicant Holder Full Name: SUN PHARMA INDUSTRIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information